CN108456926B - Method for growing crystal fiber core in crystal cladding - Google Patents
Method for growing crystal fiber core in crystal cladding Download PDFInfo
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- CN108456926B CN108456926B CN201810163892.5A CN201810163892A CN108456926B CN 108456926 B CN108456926 B CN 108456926B CN 201810163892 A CN201810163892 A CN 201810163892A CN 108456926 B CN108456926 B CN 108456926B
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- 239000013078 crystal Substances 0.000 title claims abstract description 88
- 238000005253 cladding Methods 0.000 title claims abstract description 29
- 238000000034 method Methods 0.000 title claims abstract description 25
- 239000000835 fiber Substances 0.000 title abstract description 30
- 239000002994 raw material Substances 0.000 claims abstract description 11
- 238000010438 heat treatment Methods 0.000 claims abstract description 8
- 238000002109 crystal growth method Methods 0.000 claims abstract description 6
- 230000009471 action Effects 0.000 claims abstract description 5
- 238000001816 cooling Methods 0.000 claims abstract description 5
- 230000005484 gravity Effects 0.000 claims abstract description 5
- 238000003672 processing method Methods 0.000 claims abstract description 5
- 238000004080 punching Methods 0.000 claims abstract description 5
- 239000000155 melt Substances 0.000 claims abstract description 3
- 238000002844 melting Methods 0.000 claims abstract description 3
- 230000008018 melting Effects 0.000 claims abstract description 3
- 239000013307 optical fiber Substances 0.000 claims description 27
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 4
- -1 rare earth ions Chemical class 0.000 claims description 4
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 4
- 229910052741 iridium Inorganic materials 0.000 claims description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 2
- 239000011159 matrix material Substances 0.000 claims description 2
- 229910052697 platinum Inorganic materials 0.000 claims description 2
- 229910052702 rhenium Inorganic materials 0.000 claims description 2
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 claims description 2
- 238000009826 distribution Methods 0.000 abstract description 3
- JNDMLEXHDPKVFC-UHFFFAOYSA-N aluminum;oxygen(2-);yttrium(3+) Chemical compound [O-2].[O-2].[O-2].[Al+3].[Y+3] JNDMLEXHDPKVFC-UHFFFAOYSA-N 0.000 description 19
- 229910019901 yttrium aluminum garnet Inorganic materials 0.000 description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
- 239000010453 quartz Substances 0.000 description 12
- 238000004321 preservation Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 3
- 230000017525 heat dissipation Effects 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 230000000670 limiting effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000005057 refrigeration Methods 0.000 description 2
- 229910052594 sapphire Inorganic materials 0.000 description 2
- 239000010980 sapphire Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 230000002411 adverse Effects 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 230000003321 amplification Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000004093 laser heating Methods 0.000 description 1
- 230000028161 membrane depolarization Effects 0.000 description 1
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
- C30B29/10—Inorganic compounds or compositions
- C30B29/16—Oxides
- C30B29/22—Complex oxides
- C30B29/28—Complex oxides with formula A3Me5O12 wherein A is a rare earth metal and Me is Fe, Ga, Sc, Cr, Co or Al, e.g. garnets
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B15/00—Single-crystal growth by pulling from a melt, e.g. Czochralski method
- C30B15/08—Downward pulling
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01S—DEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
- H01S3/00—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range
- H01S3/05—Construction or shape of optical resonators; Accommodation of active medium therein; Shape of active medium
- H01S3/06—Construction or shape of active medium
- H01S3/063—Waveguide lasers, i.e. whereby the dimensions of the waveguide are of the order of the light wavelength
- H01S3/067—Fibre lasers
- H01S3/06708—Constructional details of the fibre, e.g. compositions, cross-section, shape or tapering
- H01S3/06716—Fibre compositions or doping with active elements
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- Inorganic Chemistry (AREA)
- Plasma & Fusion (AREA)
- Optics & Photonics (AREA)
- Lasers (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
Abstract
The invention relates to a method for growing a crystal fiber core in a crystal cladding, which comprises the following steps: (1) adopting a microporous crystal growth method to obtain a microporous crystal with the length of 40-160mm, wherein the inner diameter of the microporous crystal is less than or equal to 1mm, or punching a hole in the center of a crystal rod by using a mechanical processing method to obtain a microporous crystal with micropores; (2) installing the microporous crystal obtained in the step (1) on a seed crystal rod of a micro-pull-down furnace; (3) 1-2g of raw materials are filled in the crucible; (4) heating and melting the raw materials in the crucible; (5) the seed rod rises to enable the microporous crystal to contact the small hole at the bottom of the crucible, and the melt in the crucible enters the hole of the microporous crystal under the action of gravity and capillary; (6) the temperature of the heater is controlled to be reduced to the room temperature at the cooling rate of 100-. Compared with the prior art, the invention enables the crystal core and the crystal cladding to be connected seamlessly, obtains uniform refractive index distribution, and thus can obtain a high-power crystal fiber laser.
Description
Technical Field
The invention belongs to the technical field of crystal material preparation, and relates to a manufacturing process of a high-power fiber laser fiber and a cladding.
Background
Quartz optical fiber has made a remarkable contribution in optical communication, and some people want to use it as a high-power laser to solve the problem of thermal effect faced by the current high-power laser, which causes thermal depolarization, thermal diffraction loss and other problems, which seriously affects the main performance indexes of the laser, such as output power, conversion efficiency and beam quality, and even causes the damage of gain medium in serious cases, and is the most main limiting factor of the high-power laser performance. To mitigate the effects of thermal effects, those skilled in the relevant art have resorted toThe gain media in the forms of slats, DISK, optical fibers and the like increase the surface area to volume ratio of the gain media, greatly improve the heat dissipation efficiency and greatly promote the power output capability of the laser. Compared with slab and DISK lasers, fiber lasers have the following advantages: the pumping structure is simpler; the limiting effect of the structure of the optical fiber on the mode makes the optical fiber have obvious advantages in the aspect of beam quality; the optical fiber coupling output can be adopted, and the application environment adaptability is good; based on these advantages, fiber lasers have become one of the major development directions of high power lasers. However, one significant obstacle to the development of high power fiber lasers is that the thermal conductivity of the quartz glass, which is currently widely used as the substrate for active optical fibers, is very low, only 1.4-1.6Wm-1K-1And the small heat conductivity coefficient brings huge adverse effect on heat dissipation, so that the high-power operation of the fiber laser still has higher requirement on refrigeration, and the continuous improvement of the power of the fiber laser is limited. For a single crystal laser gain medium, the heat conductivity coefficient of a common laser crystal Yttrium Aluminum Garnet (YAG) crystal is 14Wm-1K-1The thermal conductivity of Yttrium Aluminate (YAP) crystal is over 11Wm-1K-1Several times higher than quartz glass; therefore, the single crystal can be considered as the substrate of the active optical fiber, the heat dissipation performance of the optical fiber is improved by utilizing the high heat conductivity coefficient of the single crystal, the requirement of the system on refrigeration is reduced, the complexity of the system is simplified, and the output performance indexes of the laser, such as power, beam quality and the like, are improved. At present, mature technologies are used for growing single crystal optical fibers, including a mode guide method, a micro-pulling-down method, a laser pedestal heating method and the like, the diameter of the grown single crystal optical fiber is at least 20 micrometers, and concentrated sulfuric acid and concentrated phosphoric acid are used for corroding the optical fiber at Virginia university, so that a sapphire optical fiber with the diameter of 800nm is obtained.
Almost all optical fibers, however, require cladding, not only to confine the light beam within the fiber, but also to isolate the fiber from the surrounding environment to maintain fiber integrity, which can also be used to increase the strength of the fiber, for quartz optical fiber, the optical fiber cladding is made by sheathing quartz tube and quartz fiber core together to make prefabricated rod, co-draw in a fiber draw tower, because the quartz after heating to soften has a softened state between solid and liquid states, the dopant that has been incorporated into the core does not diffuse, maintaining the refractive index profile in the original preform, whereas for crystalline fibers, since the crystal is in a liquid state after being melted and can be freely diffused, ions doped in the core rod can be diffused into the tube rod, and the tube rod as the optical fiber cladding does not allow the doped ions to exist, the method for manufacturing the quartz cladding is not advisable. At home and abroad, no substantial progress is made in trying to prepare the crystal optical fiber cladding by sol-gel, because the efficiency of sol-gel is too low, the cladding with the thickness of 5 microns is prepared after 10 times of sol-gel, the distance from the finally available thickness of 200 microns and 300 microns is very far, and the cladding prepared by sol-gel is easy to crack. At present, no mature process report of the crystal cladding of the crystal optical fiber is available at home and abroad, a crystal core and a quartz cladding are adopted, the crystal core is manufactured in a quartz tube by a common-pulling laser base heating method, good beam quality is obtained, but the amplification of laser power does not play a great role, US ArmyResearch Laboratory and ONYX Optics company turns to research on planar guided waves, namely, a core rod and the cladding are made into square cross sections, and the core and the cladding are tightly attached by a thermal bonding mode, so that the full crystal optical fiber is really achieved, but the process qualification rate of the thermal bonding is not high.
Disclosure of Invention
The invention aims to overcome the defects of the prior art and provide a method for growing a crystal fiber core in a crystal cladding, which can ensure the complete interface between the fiber core and the cladding and ensure the uniformity of refractive index distribution.
The purpose of the invention can be realized by the following technical scheme: a method for growing a core of a crystal optical fiber in a crystal cladding, comprising the steps of:
(1) adopting a microporous crystal growth method to obtain a microporous crystal with the length of 40-160mm, wherein the inner diameter of the microporous crystal is less than or equal to 1mm, or punching a hole in the center of a crystal rod by using a mechanical processing method to obtain a microporous crystal with micropores;
(2) installing the microporous crystal obtained in the step (1) on a seed crystal rod of a micro-pull-down furnace;
(3) 1-2g of raw materials are filled in the crucible;
(4) heating and melting the raw materials in the crucible;
(5) the seed rod rises to enable the microporous crystal to contact the small hole at the bottom of the crucible, and the melt in the crucible enters the hole of the microporous crystal under the action of gravity and capillary;
(6) the temperature of the heater is controlled to be reduced to the room temperature at the cooling rate of 100-.
The microporous crystal growth method in the step (1) is a growth method for growing microporous sapphire crystals by a guided mode method described in patent application 201410765560.6.
The crucible used in the step (3) is made of iridium, platinum or rhenium.
The raw material in the crucible in the step (3) is the same as the microporous crystal matrix and is doped with rare earth ions with 0.05 to 50 atomic percent.
The length of the rear heater is 40-160 mm.
Compared with the prior art, the solution of the crystal core cladding crystal cladding of the invention, namely the method for growing the fiber core in the crystal cladding, avoids the generation of thermal stress when working at high temperature because the crystal core and the cladding are made of the same material and have consistent thermal expansion coefficients, and ensures that the refractive index difference between the fiber core and the cladding is less than 10 by controlling the concentration of the doped ions to regulate and control the refractive index value of the fiber core-3The crystal fiber with ultralow numerical aperture can be obtained, so that good laser beam quality is ensured, and because the heat flowing into the inner hole of the crystal cladding in the crucible is not enough to melt the inner wall of the transistor, the complete interface between the fiber core and the cladding can be ensured, the uniformity of refractive index distribution is ensured, the real full-crystal fiber laser is realized, and the output power of a single fiber is hopefully improved to 50 kw.
Drawings
FIG. 1 is a schematic view of the growth process in a micro-downdraw furnace of the present invention.
Detailed Description
The invention is described in detail below with reference to the figures and specific embodiments.
Example 1
The utility model provides an all-crystal fiber and covering preparation technology has adopted as the little lower stove device that draws shown in figure 1, including the heat preservation 1 that the furnace body lateral wall set up, the induction coil 2 that sets up outside the heat preservation 1, the quartz support column 9 of setting in the furnace body bottom, quartz support column 9 top is equipped with heater 3, and inside is equipped with seed rod 8, and seed rod 8 is installed and is passed heater 3 to the transistor to set up observation window 5 in back heater 7 and the same high position department of heat preservation 1.
The method for manufacturing the full-crystal optical fiber and the cladding by adopting the device comprises the following specific steps:
(1) obtaining pure YAG microporous crystal 6 with the length of 40-160mm by adopting a microporous crystal growth method, wherein the inner diameter of the microporous crystal is less than or equal to 1mm, or punching a hole in the center of a pure YAG crystal rod by adopting a mechanical processing method to obtain the pure YAG microporous crystal 6 with micropores;
(2) mounting the pure YAG microporous crystal 6 obtained in the step 1 on a seed rod 8 of a micro-pull-down furnace;
(3) filling 1-2g of rare earth ion doped YAG raw material into the crucible;
(4) heating to melt the YAG raw material in the crucible;
(5) the seed crystal rod 8 rises to enable the pure YAG microporous crystal 6 to contact a small hole at the bottom of the crucible, and the YAG melt 4 in the crucible enters the hole of the microporous crystal under the action of gravity and capillary;
(6) the temperature of the post-heater 7 is controlled to be reduced to the room temperature at the cooling rate of 100-.
Example 2
The utility model provides an all-crystal fiber and covering preparation technology has adopted as the little lower stove device that draws shown in figure 1, including the heat preservation 1 that the furnace body lateral wall set up, the induction coil 2 that sets up outside the heat preservation 1, the quartz support column 9 of setting in the furnace body bottom, quartz support column 9 top is equipped with heater 3, and inside is equipped with seed rod 8, and seed rod 8 is installed and is passed heater 3 to the transistor to set up observation window 5 in back heater 7 and the same high position department of heat preservation 1.
The method for manufacturing the full-crystal optical fiber and the cladding by adopting the device comprises the following specific steps:
(1) obtaining pure YAG microporous crystals with the length of 40-160mm by adopting a microporous crystal growth method, wherein the inner diameter of the microporous crystals is less than or equal to 1mm, or punching holes in the centers of pure YAG crystal rods by using a mechanical processing method to obtain YAG transistors with micropores;
(2) growing rare earth ion doped optical fiber with diameter smaller than the inner diameter of the microporous crystal by a mode guide method or a micro-pulling down method or a laser heating base method;
(3) inserting the crystal fiber obtained in the second step into the microporous crystal obtained in the first step, wherein a gap of 0.01-0.2mm is formed between the two crystals;
(4) filling 1-2g of pure YAG raw material into a crucible;
(5) the pure YAG microporous crystal and the crystal optical fiber obtained in the step (3) are assembled and installed on a seed crystal rod of a micro-down-draw furnace; heating to melt the YAG raw material in the crucible;
(6) the seed rod rises to enable the YAG microporous crystal and the optical fiber to be combined and contacted with the small hole at the bottom of the crucible, and the YAG melt 4 in the crucible enters a gap between the microporous crystal and the optical fiber under the action of gravity and capillary;
(7) the temperature of the post-heater 7 is controlled to be reduced to the room temperature at the cooling rate of 100-.
Claims (4)
1. A method for growing a core of a crystal optical fiber in a crystal cladding, comprising the steps of:
(1) adopting a microporous crystal growth method to obtain a microporous crystal with the length of 40-160mm, wherein the inner diameter of the microporous crystal is less than or equal to 1mm, or punching a hole in the center of a crystal rod by using a mechanical processing method to obtain a microporous crystal with micropores;
(2) installing the microporous crystal obtained in the step (1) on a seed crystal rod of a micro-pull-down furnace;
(3) 1-2g of raw materials are filled in the crucible;
(4) heating and melting the raw materials in the crucible;
(5) the seed rod rises to enable the microporous crystal to contact the small hole at the bottom of the crucible, and the melt in the crucible enters the hole of the microporous crystal under the action of gravity and capillary;
(6) the temperature of the heater is controlled to be reduced to the room temperature at the cooling rate of 100-.
2. The method of claim 1, wherein the crucible used in step (3) is made of iridium, platinum or rhenium.
3. The method of claim 1, wherein the feedstock and the microporous crystalline matrix in the crucible of step (3) are the same and are doped with rare earth ions at an atomic concentration of 0.05% to 50%.
4. The method of claim 1, wherein the afterheater has a length of 40-160 mm.
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CN109518270B (en) * | 2018-10-10 | 2021-03-26 | 同济大学 | Cladding preparation method of single crystal optical fiber |
WO2022052077A1 (en) * | 2020-09-14 | 2022-03-17 | 南京同溧晶体材料研究院有限公司 | Rare earth doped bismuth germanate single crystal optical fiber and cladding method |
CN112626611A (en) * | 2020-12-11 | 2021-04-09 | 中国科学院长春应用化学研究所 | Crucible for growing bendable flexible rare earth single crystal optical fiber and method for growing bendable flexible rare earth single crystal optical fiber by micro-pulling-down method |
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